| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01392 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:55487120-55488390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:55487917-55487936 | TGGCGCCCTCTGCTGGTCT | - | 7.51 | | EWSR1-FLI1 | MA0149.1 | chr1:55488016-55488034 | TATTCCTTCCTTCCTCCC | - | 7.54 | | EWSR1-FLI1 | MA0149.1 | chr1:55488020-55488038 | CCTTCCTTCCTCCCTTCC | - | 9.6 | | ZNF263 | MA0528.1 | chr1:55487392-55487413 | GGAAGAGAGGGGAGGAGAGGA | + | 6.02 | | ZNF263 | MA0528.1 | chr1:55488012-55488033 | TCCCTATTCCTTCCTTCCTCC | - | 6.04 | | ZNF263 | MA0528.1 | chr1:55488004-55488025 | TCCCTCTCTCCCTATTCCTTC | - | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I055021 | chr1 | 55487341 | 55488393 |
|
Enhancer Sequence | CCACCGTGCC CGGCCTGCAT TTTGTTTTTT TAGGGTGGAA GAGATCTGAG CGTGCTGAGA 60
GGCTGGCAGG AAAAAGGGTG AGTAAGCCTT GATGTGTACA AAAGAGAGAC AGAGAGAGCC 120
AGGCAGACAT GTCAGAGAAC AGCAACAGCT CTTCCCTTTA AGCCGGCAGG GAGTGGGGAC 180
ATACAGGGTG GAGAGGGGCT GCCTGTGGCA GGTGCCAGGA AGACCCCAGT GGCCTCCTTT 240
TCTCCATGAA GTGGCAGACA AGGGGCTTCC TGGGAAGAGA GGGGAGGAGA GGAGAGGGTG 300
GAGACTGGTG ATGTGCATTG GGCCCAGAGC CATTCTTGAG CAGGTGGAGA GGAAAGCATT 360
TTTGAGGCCG GCGTGCTGGT CATGACCCTC TTTTGTTCAG AATCTCCCAG AGTCCCCTAA 420
CCTCAGGAGA GGGCCATGCC TTGGCCTCGA GAGGCGTTAA AAACCAGCCT CCCATCTCAG 480
TGTCTCCAGC TGGGCCATGC ACTGCTTCCT ACCACCATTA TAACTGGACC ACAGATCCCG 540
AGCTGCCACC TCCAGGAAGC CGGCCCGGAT TCAGTGCCCA TCTGACTGAG TTCCCGCAGC 600
ACCTAGCCTG TCCCTTCTGT GAGACTTGGC TCCTCTTGCC TCCTATCACA GTCGCCTGTG 660
CTCTCATCTG CCTCCCTGTG GACTCTGAGG ATGAGGCGAG GGCTGATTCA GCTCAGGGGT 720
GAGAGCAGGT GCCAGCAGCT TATGGGCTGG GCCGGGCCTG GGCAGTGGGC AGGCCGTGGG 780
CTCAGATGAC AGGTACCTGG CGCCCTCTGC TGGTCTAGCT GGGCAAGGCT GCTGCTCCAG 840
AGTGGCCGGA AGCTTCCTGG GAGAGGCCTG GTTCTCTGGG CCTGTCCCTC TCTCCCTATT 900
CCTTCCTTCC TCCCTTCCTG AAACTGCGTC CTCCAAATCC TGCTCCAGCA CCAGCAACCC 960
CCTGCTTTTC AACAGCCTCT GGCAGCGTTT CGGTCCCTTT CTGGCCTTGA CTGGAAGGCC 1020
CCTGTCCCCC AAGGACACTG CTGCCGTCCC TGCAGTCCTT TCCCCCCGCC TGAGAGGGGT 1080
AGGGTCTCCT TGCTCTCAGT GCCCCACTCT CTGGATCATT GTCCTTCTCT CCTCCATAAA 1140
CGCAGTCATG CGCCACACAG CAATGTTTCA GGCAACGACA GACCACATAC ATGACAGTGG 1200
TTCCATAAGA TTACAACAGA GCTGAGAAAC TCCTGTCACC TCGCTTAGAG ACGTCATAGC 1260
TGTCAGGCCT 1270
|
